CA2194563A1 - Derives heterocycliques anti-helicobacter d'azolones - Google Patents

Derives heterocycliques anti-helicobacter d'azolones

Info

Publication number
CA2194563A1
CA2194563A1 CA002194563A CA2194563A CA2194563A1 CA 2194563 A1 CA2194563 A1 CA 2194563A1 CA 002194563 A CA002194563 A CA 002194563A CA 2194563 A CA2194563 A CA 2194563A CA 2194563 A1 CA2194563 A1 CA 2194563A1
Authority
CA
Canada
Prior art keywords
4alkyl
pyridinyl
formula
optionally substituted
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002194563A
Other languages
English (en)
Inventor
Jan Heeres
Raymond Antoine Stokbroekx
Marc Willems
Robert Jozef Maria Hendrickx
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Janssen Pharmaceutica NV
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of CA2194563A1 publication Critical patent/CA2194563A1/fr
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Polymerization Catalysts (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)

Abstract

L'invention concerne des composés de formule (I), leurs sels d'addition pharmaceutiquement acceptables et leurs formes stéréochimiquement isomériques. Dans cette formule, Y est CH ou bien N; R?1¿, R?2¿ et R?3¿ sont chacun indépendamment hydrogène ou alkyle C¿1-4?; R?4¿ et R?5¿ sont chacun indépendamment hydrogène, halo, alkyle C¿1-4?, alkyloxy C¿1-4?, hydroxy, trifluorométhyle, trifluorométhyloxy ou difluorométhyloxy; R?6¿ est pyridinyle éventuellement substitué avec jusqu'à deux groupes alkyle C¿1-4?; di(alkyle C¿1-4?)hydroxypyridinyle; di(alkyle C¿1-4?)alkyloxypyridinyle C¿1-4?; pyridazinyle éventuellement substitué avec alkyloxy C¿1-4?; pyrimidinyle éventuellement substitué avec hydroxy ou alkyloxy C¿1-4?; thiazolyle éventuellement substitué avec alkyle C¿1-4?; thiadiazolyle éventuellement substitué avec alkyle C¿1-4?; benzoxazolyle ou benzothiazolyle; ou bien R?6¿ est pyrazinyle ou pyridazinyle substitué avec alkyle C¿1-4?; Z est C=O ou CHOH; et (a) est un radical de formule (a-1), (a-2), (a-3), (a-4), (a-5), (a-6), ou bien (a-7). L'invention concerne également des compositions comprenant lesdits composés, des procédés pour les préparer et l'utilisation de ces composés comme médicament.
CA002194563A 1994-07-12 1995-07-05 Derives heterocycliques anti-helicobacter d'azolones Abandoned CA2194563A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP94202018.1 1994-07-12
EP94202018 1994-07-12
PCT/EP1995/002616 WO1996001821A1 (fr) 1994-07-12 1995-07-05 Derives heterocycliques anti-helicobacter d'azolones

Publications (1)

Publication Number Publication Date
CA2194563A1 true CA2194563A1 (fr) 1996-01-25

Family

ID=8217031

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002194563A Abandoned CA2194563A1 (fr) 1994-07-12 1995-07-05 Derives heterocycliques anti-helicobacter d'azolones

Country Status (20)

Country Link
US (1) US5607932A (fr)
EP (1) EP0770073A1 (fr)
JP (1) JPH10502383A (fr)
CN (1) CN1067999C (fr)
AU (1) AU684986B2 (fr)
BR (1) BR9508380A (fr)
CA (1) CA2194563A1 (fr)
CZ (1) CZ2697A3 (fr)
FI (1) FI970110A (fr)
HU (1) HUT76641A (fr)
IL (1) IL114534A (fr)
MX (1) MX9700338A (fr)
MY (1) MY131785A (fr)
NO (1) NO310289B1 (fr)
NZ (1) NZ290116A (fr)
PL (1) PL318142A1 (fr)
RU (1) RU2152940C1 (fr)
SK (1) SK2197A3 (fr)
WO (1) WO1996001821A1 (fr)
ZA (1) ZA955753B (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100411190B1 (ko) * 1995-12-26 2004-03-26 에스케이케미칼주식회사 에틸렌글리콜의회수방법
KR20000005291A (ko) 1996-06-25 2000-01-25 다케다 야쿠힌 고교 가부시키가이샤 옥사졸론 유도체 및 항-헬리코박터 파일로리 제제로서의 이의용도
WO1997049703A2 (fr) * 1996-06-25 1997-12-31 Takeda Chemical Industries, Ltd. DERIVES DE L'OXAZOLONE ET LEUR UTILISATION EN TANT QU'AGENT ANTI-$i(HELICOBACTER PYLORI)
CN101083992A (zh) 2004-09-20 2007-12-05 泽农医药公司 抑制人硬脂酰CoA去饱和酶的哒嗪衍生物
TW200626138A (en) 2004-09-20 2006-08-01 Xenon Pharmaceuticals Inc Heterocyclic derivatives and their use as therapeutic agents
CA2580787A1 (fr) 2004-09-20 2006-03-30 Xenon Pharmaceuticals Inc. Derives heterocycliques et utilisation de ceux-ci comme agents therapeutiques
AR051092A1 (es) 2004-09-20 2006-12-20 Xenon Pharmaceuticals Inc Derivados heterociclicos y su uso como inhibidores de la estearoil-coa
MX2007003327A (es) 2004-09-20 2007-06-05 Xenon Pharmaceuticals Inc Derivados heterociclicos, y su uso como mediadores de estearoil-coa desaturasa.
AU2005286648A1 (en) 2004-09-20 2006-03-30 Xenon Pharmaceuticals Inc. Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors
EP2269610A3 (fr) 2004-09-20 2011-03-09 Xenon Pharmaceuticals Inc. Dérivés hétérocycliques et leur utilisation en tant qu'inhibiteurs de la stearoyl-coa desaturase
CA2618646A1 (fr) 2005-06-03 2007-11-15 Xenon Pharmaceuticals Inc. Derives aminothiazole utilises en tant qu'inhibiteurs de la stearoyle-coa desaturase humaine
MX2010014572A (es) 2008-06-27 2011-03-24 Novartis Ag Compuestos organicos.
EP2852589B1 (fr) * 2012-05-22 2021-04-28 Autifony Therapeutics Limited Triazoles en tant qu'inhibiteurs de kv3
EP3464262B1 (fr) * 2016-05-27 2020-02-26 Bristol-Myers Squibb Company Utilisation de triazolones et de tétrazolones comme inhibiteurs de la voie de signalisation rho/rock

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4791111A (en) * 1985-12-23 1988-12-13 Janssen Pharmaceutica, N.V. [[4-[4-(4-phenyl-1-piperazinyl)phenoxymethyl]-1,3-dioxolan-2-yl]methyl]-1H-imidazoles and 1H-1,2,4-triazoles having anti-microbial properties
CA1331757C (fr) * 1988-02-29 1994-08-30 Janssen Pharmaceutica Naamloze Vennootschap 5-lipoxygenase inhibant les 4-(4-phenyl-1-piperazinyl)phenols
CA2076257A1 (fr) * 1991-09-13 1993-03-14 Jan Heeres Derives de 4-{4-¬4-(4-hydroxyphenyl)-1-piperazinyl|phenyl}-5-methyl-3h-1,2,4-triazol-3-one
TW279864B (fr) * 1993-02-19 1996-07-01 Janssen Pharmaceutica Nv

Also Published As

Publication number Publication date
IL114534A (en) 1999-08-17
RU2152940C1 (ru) 2000-07-20
SK2197A3 (en) 1997-11-05
EP0770073A1 (fr) 1997-05-02
HUT76641A (en) 1997-10-28
AU3075595A (en) 1996-02-09
NO970086D0 (no) 1997-01-09
FI970110A0 (fi) 1997-01-10
JPH10502383A (ja) 1998-03-03
MY131785A (en) 2007-08-30
NZ290116A (en) 1997-11-24
CN1152310A (zh) 1997-06-18
IL114534A0 (en) 1995-11-27
NO970086L (no) 1997-03-10
CZ2697A3 (en) 1997-09-17
ZA955753B (en) 1997-01-11
PL318142A1 (en) 1997-05-12
BR9508380A (pt) 1997-12-23
HU9700077D0 (en) 1997-02-28
FI970110A (fi) 1997-01-10
CN1067999C (zh) 2001-07-04
MX9700338A (es) 1997-05-31
AU684986B2 (en) 1998-01-08
US5607932A (en) 1997-03-04
NO310289B1 (no) 2001-06-18
WO1996001821A1 (fr) 1996-01-25

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Legal Events

Date Code Title Description
FZDE Discontinued